Aguilera Paula, López-Contreras Andrés J
Centro Andaluz de Biología Molecular y Medicina Regenerativa (CABIMER), Consejo Superior de Investigaciones Científicas (CSIC), Universidad de Sevilla - Universidad Pablo de Olavide, Seville, Spain.
Trends Genet. 2023 Jun;39(6):505-519. doi: 10.1016/j.tig.2023.02.009. Epub 2023 Mar 7.
ATRX (alpha-thalassemia mental retardation X-linked) is one of the most frequently mutated tumor suppressor genes in human cancers, especially in glioma, and recent findings indicate roles for ATRX in key molecular pathways, such as the regulation of chromatin state, gene expression, and DNA damage repair, placing ATRX as a central player in the maintenance of genome stability and function. This has led to new perspectives about the functional role of ATRX and its relationship with cancer. Here, we provide an overview of ATRX interactions and molecular functions and discuss the consequences of its impairment, including alternative lengthening of telomeres and therapeutic vulnerabilities that may be exploited in cancer cells.
ATRX(X连锁α地中海贫血伴智力发育迟缓)是人类癌症中最常发生突变的肿瘤抑制基因之一,尤其是在神经胶质瘤中。最近的研究结果表明,ATRX在关键分子途径中发挥作用,如染色质状态调控、基因表达和DNA损伤修复,这使ATRX成为维持基因组稳定性和功能的核心因素。这为ATRX的功能作用及其与癌症的关系带来了新的视角。在此,我们概述了ATRX的相互作用和分子功能,并讨论了其功能受损的后果,包括端粒的替代延长以及癌细胞中可能被利用的治疗弱点。